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The official name of this gene is “cytochrome b-245, beta polypeptide.”
CYBB is the gene's official symbol. The CYBB gene is also known by other names, listed below.
The CYBB gene provides instructions for making a protein called cytochrome b-245, beta subunit (also known as p91-phox). This protein is one part (subunit) of a group of proteins that forms an enzyme complex called NADPH oxidase, which plays an essential role in the immune system. Within this complex, the cytochrome b-245, beta subunit has an alpha subunit partner (produced from the CYBA gene). Both alpha and beta subunits are required for either to function and the NADPH oxidase complex requires both subunits in order to be functional. NADPH oxidase is primarily active in immune system cells called phagocytes. These cells catch and destroy foreign invaders such as bacteria and fungi. NADPH oxidase is also thought to regulate the activity of immune cells called neutrophils. These cells play a role in adjusting the inflammatory response to optimize healing and reduce injury to the body.
The presence of foreign invaders stimulates phagocytes and triggers the assembly of NADPH oxidase. This enzyme participates in a chemical reaction that converts oxygen to a toxic molecule called superoxide. Superoxide is used to generate several other compounds, including hydrogen peroxide (a strong disinfectant) and hypochlorous acid (the active ingredient in bleach). These highly reactive, toxic substances are known as reactive oxygen species. Phagocytes use these substances to kill foreign invaders, preventing them from reproducing in the body and causing illness.
The CYBB gene belongs to a family of genes called CYB (cytochrome b).
A gene family is a group of genes that share important characteristics. Classifying individual genes into families helps researchers describe how genes are related to each other. For more information, see What are gene families? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genefamilies) in the Handbook.
More than 650 mutations in the CYBB gene have been found to cause chronic granulomatous disease. People with this disorder are at increased risk of developing recurrent episodes of infection and inflammation due to a weakened immune system. Mutations in the CYBB gene cause approximately 70 percent of all cases of this condition. Most of these mutations change single building blocks of protein (amino acids) in the cytochrome b-245, beta subunit or cause it to be abnormally short and nonfunctional. An altered protein not only diminishes the function of the beta subunit, but the function of its alpha subunit partner as well. Without these subunits, NADPH oxidase cannot assemble or function properly. As a result, phagocytes are unable to produce reactive oxygen species to kill foreign invaders, and neutrophil activity is not regulated. A lack of NADPH oxidase leaves affected individuals vulnerable to many types of infection and excessive inflammation.
Cytogenetic Location: Xp21.1
Molecular Location on the X chromosome: base pairs 37,780,016 to 37,813,464
The CYBB gene is located on the short (p) arm of the X chromosome at position 21.1.
More precisely, the CYBB gene is located from base pair 37,780,016 to base pair 37,813,464 on the X chromosome.
See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.
You and your healthcare professional may find the following resources about CYBB helpful.
You may also be interested in these resources, which are designed for genetics professionals and researchers.
See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.
acids ; bacteria ; chronic ; enzyme ; gene ; granulomatous ; hydrogen peroxide ; hypochlorous acid ; immune system ; infection ; inflammation ; injury ; molecule ; neutrophils ; oxidase ; oxygen ; phagocytes ; protein ; reactive oxygen species ; subunit ; toxic
You may find definitions for these and many other terms in the Genetics Home Reference Glossary (/glossary).
The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.